Partnering Solutions
-
Advarra Regulatory Consulting
6/10/2021
Our regulatory consultants take action and move your research forward. If you’re looking for help in the development of innovative life science and digital health products, then Advarra® is the answer.
-
An Introductory Guide To Clinical EU Qualified Person (QP) Services
10/3/2022
PCI's team of qualified persons assume responsibility for all stages of the process, safeguarding patients including the audit of the supply chain for GMP compliance in addition to certification of products for use in clinical trials.
-
How To Achieve Timely Migration Of Your TMF
9/18/2023
This precise, proven methodology delivers a high-quality migration of your Trial Master File to the destination system, typically just 4-6 weeks after receiving all documents from the source system.
-
Clinical And Regulatory Strategy
11/7/2023
Many biotechnology companies come to Australia to conduct early phase clinical trials and take advantage of straightforward regulatory streams and of the lucrative 43.5% R&D cash refund scheme. Biotechnology companies then often look at locations in Asia, such as South Korea, Thailand and China to tap into their huge treatment-naïve patient populations for their later phase clinical research.
-
Modernize Operations To Support A New Way Forward For Clinical Trials With Cognizant® SIP
6/29/2020
Cognizant Shared Investigator Platform (SIP) is a robust platform that transforms how sponsors and sites collaborate throughout key components of the clinical trial life cycle.
-
Inspection Readiness
10/30/2023
Learn how your company can enable productive interactions with inspectors through Inspection Readiness (IR) gap assessments, and propel to the next phase of development.
-
Pharmacometric Services
6/27/2023
Our talented and experienced team can assist in all Clinical Study Phases (Phase 0, I, II and III) and in study designs ranging from First in Human (FIH), Single Ascending Dose (SAD), Multiple Ascending Dose (MAD), Drug-Drug Interaction (DDI), Bioavailability/Bioequivalence (BA/BE), Food Effect as well as Special Population studies.
-
Packaging Design And Development Services
2/27/2024
We are manufacturing, packaging, and supply chain experts, harnessing experience and expertise to deliver you a seamless solution with the ultimate aim of improving the lives of patients.
-
Expert Travel Solution For Clinical Trial Participants
7/15/2019
Getting participants to and from a research site can be burdensome for the site staff, study coordinators, participants, and their families and/or caregivers. Greenphire has designed the most comprehensive travel solution built to meet the retention goals of global clinical research.
-
GMO Solutions
6/27/2023
Novotech initiated the first national, privately owned, commercial Institutional Biosafety Committee (IBC) in Australia, successfully accredited by the Australian Office of the Gene Technology Regulator (OGTR).